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  • shi
    replied
    Originally posted by GenoMax View Post
    @Wei: Any update on adding support for SAM v.1.4 tags to featureCounts?
    Hi @GenoMax, could you be more specific on what tags you'd like featureCounts to support?

    Leave a comment:


  • dpryan
    replied
    Originally posted by shi View Post
    It is written in C (not C++ or java).
    I knew I should have looked this up... :P

    Leave a comment:


  • GenoMax
    replied
    Originally posted by shi View Post
    It is written in C (not C++ or java).
    @Wei: Any update on adding support for SAM v.1.4 tags to featureCounts?

    Leave a comment:


  • susanklein
    replied
    featureCounts works great. Thanks for the tip.

    Leave a comment:


  • shi
    replied
    Originally posted by dpryan View Post
    featureCounts is part of the subRead package, which is written in either java or C++ (I'd have to look). We script this in python as well. Since it's a regular executable it's not a problem to do.
    It is written in C (not C++ or java).

    Leave a comment:


  • dpryan
    replied
    featureCounts is part of the subRead package, which is written in either java or C++ (I'd have to look). We script this in python as well. Since it's a regular executable it's not a problem to do.

    Leave a comment:


  • Michael.Ante
    replied
    It seems your bam file is encoded with v1.4, there the CIGAR string distinguishes between matches and missmatches. You can use reformat.sh from the bbmap suite in order to convert from SAM1.4 to SAM1.3. See https://www.biostars.org/p/182156/#182160 and http://seqanswers.com/forums/showthread.php?t=46174
    Last edited by Michael.Ante; 04-12-2016, 12:28 AM. Reason: typo

    Leave a comment:


  • susanklein
    replied
    which package is featureCounts from? I need to script, preferably in python, to handle a large number of bam files, so its hard to interact with R (can't script in R). I guess I will have to learn R!

    s.

    Leave a comment:


  • dpryan
    replied
    featureCounts is much faster. I'm a little surprised that htseq-count was never updated to support the = and X cigar operators.

    Leave a comment:


  • susanklein
    started a topic HTseq error

    HTseq error

    Hi,

    anyone know how to solve these cigar type errors in HTseq? Seems ti is unusable until its solved..

    python -m HTSeq.scripts.count in_sorted.bam ref.gff -f bam -s no -t CDS -m union -i locus_tag

    Error occured when reading beginning of SAM/BAM file.
    Unknown CIGAR code '=' encountered.
    [Exception type: ValueError, raised in _HTSeq.pyx:1163]

    Or better yet, another progam to get raw counts from bam and gff files. Don't say 'bedtools' because that doesn't work either.. endlessly gives '0' as all the counts.

    Thanks,

    S.

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